rs372857241

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs372857241(C;T)

Make rs372857241(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

1610586

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs372857241
dbSNP (classic)	rs372857241
ClinGen	rs372857241
ebi	rs372857241
HLI	rs372857241
Exac	rs372857241
Gnomad	rs372857241
Varsome	rs372857241
LitVar	rs372857241
Map	rs372857241
PheGenI	rs372857241
Biobank	rs372857241
1000 genomes	rs372857241
hgdp	rs372857241
ensembl	rs372857241
geneview	rs372857241
scholar	rs372857241
google	rs372857241
pharmgkb	rs372857241
gwascentral	rs372857241
openSNP	rs372857241
23andMe	rs372857241
SNPshot	rs372857241
SNPdbe	rs372857241
MSV3d	rs372857241
GWAS Ctlg	rs372857241

Max Magnitude

0

ClinVar
Risk	rs372857241(G;G) rs372857241(T;T)
Alt	rs372857241(G;G) rs372857241(T;T)
Reference	Rs372857241(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXC1
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.1610821C>G
CLNSRC
CLNACC	RCV000190252.1,